FDA.reportPublic FDA data

TOTAL PERFORMANCE ANTIBACTERIAL FOAM HAND

Manufacturer
MORGAN GALLACHER INC
Effective date
2016-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:22:05

Label at a glance#

ProductTOTAL PERFORMANCE ANTIBACTERIAL FOAM HAND
Active ingredientCHLOROXYLENOL
Label structure1 sections

Label contents#

Full prescribing information#

TOTAL PERFORMANCE ANTI-BACTERIAL FOAM HAND SOAP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Parachlorometaxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antibacterial

USES

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  •  For external Use only

​When Using this Product

OTC - WHEN USING SECTION

Avoid contact with the eyes.

In case of eye contact, fluch eyes with water. Do not Ingest

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor if irritation or redness develops

or if condition persist

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help

or contact Posion Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to wet hands.

Work into a latherand rinse thoroughly.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycerine, Aloe Vera, Sodium Chloride, DMDM Hydation, Fragrance, FD&C Yellow #5, FD&C Red #40

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50241-201-082022-12-29C16284748780-19d75b9cf-ddd2-f424-e053-dadaa90a57ceFLO-KEM TOTAL PERFORMANCE ANTI-BACTERIAL FOAM HAND
50241-201-082020-01-31C16284748780-19d75b9cf-ddd2-f424-e053-dadaa90a57ceFLO-KEM TOTAL PERFORMANCE ANTI-BACTERIAL FOAM HAND

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50241-20150241-201-08

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QACTIB
SODIUM LAURETH SULFATEBPV390UAP0IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
HYDANTOINI6208298TAIACT
GLYCERINPDC6A3C0OXIACT
FD&C RED NO. 40WZB9127XOAIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5f39d489-2f40-44bc-9a5e-6a2578294ee76deebc35-d941-4753-9dfb-45d18b7d7f832022-12-29WarningsExact identifier
spl set id: 6deebc35-d941-4753-9dfb-45d18b7d7f83

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.